A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019764



Internal ID19108982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17581412..17635573hg38UCSC Ensembl
Innerchr9:17581410..17635571hg19UCSC Ensembl
Innerchr9:17571410..17625571hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3854162
hg1954162
hg1854162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7466n100
Supporting Variantsnssv3690650
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019764
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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